Richard Warth

Regensburg, BY 93053, Germany

Last Updated: 09/26/2026

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Found 43 publications

Inhibition of (interstitial) P2Y6 receptors attenuates fibrosis progression.

Inhibition of (interstitial) P2Y6 receptors attenuates fibrosis progression.

Journal: Research square
Published: April 10, 2026

Inhibition of (interstitial) P2Y6 receptors attenuates fibrosis progression.

Inhibition of (interstitial) P2Y6 receptors attenuates fibrosis progression.

Journal: Pflugers Archiv : European journal of physiology
Published: March 18, 2026

Inhibition of (interstitial) P2Y6 receptors attenuates renal fibrosis progression.

Inhibition of (interstitial) P2Y6 receptors attenuates renal fibrosis progression.

Journal: bioRxiv : the preprint server for biology
Published: February 09, 2026

Elexacaftor/tezacaftor/ivacaftor corrects salt-wasting in cystic fibrosis.

Elexacaftor/tezacaftor/ivacaftor corrects salt-wasting in cystic fibrosis.

Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
Published: October 14, 2025

Somatic Mutations in MCOLN3 Are Associated With Aldosterone-Producing Adenomas.

Somatic Mutations in MCOLN3 Are Associated With Aldosterone-Producing Adenomas.

Journal: Hypertension (Dallas, Tex. : 1979)
Published: August 07, 2025

Somatic Mutations in MCOLN3 in Aldosterone-Producing Adenomas cause Primary Aldosteronism.

Somatic Mutations in MCOLN3 in Aldosterone-Producing Adenomas cause Primary Aldosteronism.

Journal: bioRxiv : the preprint server for biology
Published: November 01, 2024

The ex vivo perfused mouse adrenal gland-a new model to study aldosterone secretion.

The ex vivo perfused mouse adrenal gland-a new model to study aldosterone secretion.

Journal: Pflugers Archiv : European journal of physiology
Published: January 24, 2024

A missense mutation in Ehd1 associated with defective spermatogenesis and male infertility.

A missense mutation in Ehd1 associated with defective spermatogenesis and male infertility.

Journal: Frontiers in cell and developmental biology
Published: June 16, 2023

KidneyGPS: a user-friendly web application to help prioritize kidney function genes and variants based on evidence from genome-wide association studies.

KidneyGPS: a user-friendly web application to help prioritize kidney function genes and variants based on evidence from genome-wide association studies.

Journal: BMC bioinformatics
Published: February 17, 2023

Somatic SLC30A1 mutations altering zinc transporter ZnT1 cause aldosterone-producing adenomas and primary aldosteronism.

Somatic SLC30A1 mutations altering zinc transporter ZnT1 cause aldosterone-producing adenomas and primary aldosteronism.

Journal: Nature genetics
Published: July 05, 2022

EAST/SeSAME Syndrome and Beyond: The Spectrum of Kir4.1- and Kir5.1-Associated Channelopathies.

EAST/SeSAME Syndrome and Beyond: The Spectrum of Kir4.1- and Kir5.1-Associated Channelopathies.

Journal: Frontiers in physiology
Published: January 11, 2022

A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness.

A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness.

Journal: Journal of the American Society of Nephrology : JASN
Published: October 06, 2021
Showing 1-12 of 43

Last Updated: 09/26/2026